Preparation and in vitro evaluation of hydrophilic fenretinide nanoparticles-Reference-Cited by-同舟云学术

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Preparation and in vitro evaluation of hydrophilic fenretinide nanoparticles

Published:2015-02 Issue:2 Volume:479 Page:329-337
ISSN:0378-5173
Container-title:International Journal of Pharmaceutics
language:en
Short-container-title:International Journal of Pharmaceutics

Author:

Ledet Grace A.,Graves Richard A.,Glotser Elena Y.,Mandal Tarun K.,Bostanian Levon A.

Funder

National Institute of Health (NIH)

Louisiana Cancer Research Consortium (LCRC)

Publisher

Elsevier BV

Subject

Pharmaceutical Science

Reference45 articles.

1. Microfluidic preparation of liposomes to determine particle size influence on cellular uptake mechanisms;Andar;Pharm. Res.,2014

2. In vitro models to evaluate the permeability of poorly soluble drug entities: challenges and perspectives;Buckley;Eur. J. Pharm. Sci.,2012

3. Approach to improve compound recovery in a high-throughput Caco-2 permeability assay supported by liquid chromatography-tandem mass spectrometry;Cai;J. Pharm. Sci.,2012

4. Phase I trial of oral fenretinide in children with high-risk solid tumors: a report from the Children’s Oncology Group (CCG 09709);Children's Oncology Group (CCG 09709);J. Clin. Oncol.,2006

5. A phase I–II preoperative biomarker trial of fenretinide in ascitic ovarian cancer;Colombo;Cancer Epidemiol. Biomarkers Prev.,2006

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4. Preparation and Characterization of Amorphous Solid Dispersions for the Solubilization of Fenretinide;Pharmaceuticals;2023-03-02

5. Microencapsulation of amorphous solid dispersions of fenretinide enhances drug solubility and release from PLGA in vitro and in vivo;International Journal of Pharmaceutics;2020-08

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